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    NDC 70518-2626-00 Divalproex Sodium 500 mg/1 Details

    Divalproex Sodium 500 mg/1

    Divalproex Sodium is a ORAL TABLET, DELAYED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is DIVALPROEX SODIUM.

    Product Information

    NDC 70518-2626
    Product ID 70518-2626_048cf37e-3dc3-2c89-e063-6394a90a01da
    Associated GPIs
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    Proprietary Name Divalproex Sodium
    Proprietary Name Suffix n/a
    Non-Proprietary Name Divalproex Sodium
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, DELAYED RELEASE
    Route ORAL
    Active Ingredient Strength 500
    Active Ingredient Units mg/1
    Substance Name DIVALPROEX SODIUM
    Labeler Name REMEDYREPACK INC.
    Pharmaceutical Class Anti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE], Mood Stabilizer [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA079163
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-2626-00 (70518262600)

    NDC Package Code 70518-2626-0
    Billing NDC 70518262600
    Package 100 POUCH in 1 BOX (70518-2626-0) / 1 TABLET, DELAYED RELEASE in 1 POUCH (70518-2626-1)
    Marketing Start Date 2020-03-12
    NDC Exclude Flag N
    Pricing Information N/A